AU2004264668A1 - Use of acyl cyclohexandione derivatives in conjunction with ethephon for treating pomaceous fruit - Google Patents
Use of acyl cyclohexandione derivatives in conjunction with ethephon for treating pomaceous fruit Download PDFInfo
- Publication number
- AU2004264668A1 AU2004264668A1 AU2004264668A AU2004264668A AU2004264668A1 AU 2004264668 A1 AU2004264668 A1 AU 2004264668A1 AU 2004264668 A AU2004264668 A AU 2004264668A AU 2004264668 A AU2004264668 A AU 2004264668A AU 2004264668 A1 AU2004264668 A1 AU 2004264668A1
- Authority
- AU
- Australia
- Prior art keywords
- formula
- ethephon
- compound
- treatment
- pome fruit
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 title claims description 44
- 235000013399 edible fruits Nutrition 0.000 title claims description 36
- 239000005976 Ethephon Substances 0.000 title claims description 35
- -1 acyl cyclohexandione derivatives Chemical class 0.000 title description 25
- 150000001875 compounds Chemical class 0.000 claims description 37
- 238000011282 treatment Methods 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 27
- 241000196324 Embryophyta Species 0.000 claims description 21
- 230000008124 floral development Effects 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 11
- 239000007921 spray Substances 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 241000220324 Pyrus Species 0.000 claims description 7
- 235000021016 apples Nutrition 0.000 claims description 7
- 235000021017 pears Nutrition 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 6
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 159000000007 calcium salts Chemical class 0.000 claims description 3
- 244000141359 Malus pumila Species 0.000 claims 1
- NLKUPINTOLSSLD-UHFFFAOYSA-L calcium;4-(1-oxidopropylidene)-3,5-dioxocyclohexane-1-carboxylate Chemical compound [Ca+2].CCC([O-])=C1C(=O)CC(C([O-])=O)CC1=O NLKUPINTOLSSLD-UHFFFAOYSA-L 0.000 description 22
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 10
- 239000013543 active substance Substances 0.000 description 7
- 241000220225 Malus Species 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000003630 growth substance Substances 0.000 description 6
- 241001208007 Procas Species 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- 235000017788 Cydonia oblonga Nutrition 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 3
- 230000009105 vegetative growth Effects 0.000 description 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000005986 Prohexadione Substances 0.000 description 2
- 240000001987 Pyrus communis Species 0.000 description 2
- 235000014443 Pyrus communis Nutrition 0.000 description 2
- 239000005994 Trinexapac Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- JUZXDNPBRPUIOR-UHFFFAOYSA-N chlormequat Chemical compound C[N+](C)(C)CCCl JUZXDNPBRPUIOR-UHFFFAOYSA-N 0.000 description 2
- 244000038559 crop plants Species 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- NNCAWEWCFVZOGF-UHFFFAOYSA-N mepiquat Chemical compound C[N+]1(C)CCCCC1 NNCAWEWCFVZOGF-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 235000021018 plums Nutrition 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- BUCOQPHDYUOJSI-UHFFFAOYSA-N prohexadione Chemical compound CCC(=O)C1C(=O)CC(C(O)=O)CC1=O BUCOQPHDYUOJSI-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000026267 regulation of growth Effects 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- VOYADQIFGGIKAT-UHFFFAOYSA-N 1,3-dibutyl-4-hydroxy-2,6-dioxopyrimidine-5-carboximidamide Chemical group CCCCn1c(O)c(C(N)=N)c(=O)n(CCCC)c1=O VOYADQIFGGIKAT-UHFFFAOYSA-N 0.000 description 1
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- VAJZCFLYJRMBFN-UHFFFAOYSA-N 4,4-dimethylmorpholin-4-ium Chemical compound C[N+]1(C)CCOCC1 VAJZCFLYJRMBFN-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 244000298697 Actinidia deliciosa Species 0.000 description 1
- 235000009436 Actinidia deliciosa Nutrition 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000004936 Bromus mango Nutrition 0.000 description 1
- 101100234822 Caenorhabditis elegans ltd-1 gene Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000009025 Carya illinoensis Nutrition 0.000 description 1
- 244000068645 Carya illinoensis Species 0.000 description 1
- 239000005974 Chlormequat Substances 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 241001672694 Citrus reticulata Species 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000723382 Corylus Species 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241001091440 Grossulariaceae Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000758791 Juglandaceae Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000007228 Mangifera indica Species 0.000 description 1
- 235000014826 Mangifera indica Nutrition 0.000 description 1
- 239000005984 Mepiquat Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 244000183278 Nephelium litchi Species 0.000 description 1
- 235000015742 Nephelium litchi Nutrition 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 240000006711 Pistacia vera Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- 244000007021 Prunus avium Species 0.000 description 1
- 235000010401 Prunus avium Nutrition 0.000 description 1
- 241001290151 Prunus avium subsp. avium Species 0.000 description 1
- 240000002878 Prunus cerasus Species 0.000 description 1
- 235000005805 Prunus cerasus Nutrition 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 235000006029 Prunus persica var nucipersica Nutrition 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 244000017714 Prunus persica var. nucipersica Species 0.000 description 1
- 235000001537 Ribes X gardonianum Nutrition 0.000 description 1
- 235000001535 Ribes X utile Nutrition 0.000 description 1
- 235000002357 Ribes grossularia Nutrition 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000002355 Ribes spicatum Nutrition 0.000 description 1
- 240000007651 Rubus glaucus Species 0.000 description 1
- 235000009184 Spondias indica Nutrition 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 244000078534 Vaccinium myrtillus Species 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000004849 alkoxymethyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- VBQDSLGFSUGBBE-UHFFFAOYSA-N benzyl(triethyl)azanium Chemical compound CC[N+](CC)(CC)CC1=CC=CC=C1 VBQDSLGFSUGBBE-UHFFFAOYSA-N 0.000 description 1
- YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 1
- 235000021029 blackberry Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000005078 fruit development Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 229920002114 octoxynol-9 Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 235000020233 pistachio Nutrition 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000013138 pruning Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000005537 sulfoxonium group Chemical group 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Detergent Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Fertilizers (AREA)
Description
IN THE MATTER OF an Australian Application corresponding to PCT Application PCT/EP2004/008832 RWS Group Ltd, of Europa House, Marsham Way, Gerrards Cross, Buckinghamshire, England, hereby solemnly and sincerely declares that, to the best of its knowledge and belief, the following document, prepared by one of its translators competent in the art and conversant with the English and German languages, is a true and correct translation of the PCT Application filed under No. PCT/EP2004/008832. Date: 1 February 2006 S. ANTHONY Director For and on behalf of RWS Group Ltd 1 Use of acylcyclohexanedione derivatives in conjunction with ethephon for treating pomaceous fruit The present invention relates to the use of acylcyclohexanedione derivatives together 5 with ethephon for the treatment of pome fruit. Reducing excessive shoot growth by chemical means, i.e. the use of growth regulators, is desired in perennial fruit plantations since pruning costs can be avoided and crop protection measures can be made easier; moreover, light exposure inside the 10 plantation can be improved. Both acylcyclohexanedione derivatives and ethephon (2-chloroethylphosphonic acid) are known growth regulators. Thus, EP-A-123001 and EP-A-126713 describe the use of acylcyclohexanedione compounds of the formula 15 O ROOC -CO- R' 20 O in which R is hydrogen, alkyl, alkylthioalkyl or substituted or unsubstituted phenyl and R' is alkyl, substituted or unsubstituted benzyl, phenethyl, phenoxymethyl, 2-thienylmethyl, alkoxymethyl or alkylthiomethyl, 25 or their salts as growth regulators. In J. Amer. Soc. Hort. Sci. 94, pp. 11-14 (1969), L.J. Edgerton and W.J. Greenhalgh describe the growth-regulatory effect of ethephon on apples. 30 A disadvantage in the use of acylcyclohexanedione derivatives for the purposes of growth regulation which has emerged is that, in certain plants, floral development in the year after the treatment, and, as a consequence, also fruit development, is markedly reduced. Thus, D. Sugar, D.C. Elfving and E.A. Mielke report in Acta Hort. 596, pp. 757-760 (2002) that the treatment of pear trees with prohexadione-calcium leads 35 to reduced subsequent flowering. Experiments carried out by the Applicant company have confirmed these results and demonstrated that acylcyclohexanedione-based growth regulators, in particular prohexadione-calcium and to a particularly high degree trinexapac, or trinexapac-ethyl, lead to markedly reduced floral development in pome fruit and specifically in apples and pears in the year after the treatment. In the most 40 extreme case, no floral development at all takes place in the year after the treatment. Not only does the treatment lead to reduced subsequent flowering, and frequently in association therewith, reduced yields in the year in question, but it may also trigger biennial bearing. Biennial bearing means that a year with unduly low yield is followed 45 by a year with unduly high yield, usually of low quality. In perennial fruit crops such as pome fruit (apples, pears, quinces), stone fruit (sweet cherries, morello cherries, plums, 2 quetsch, peaches, nectarines, apricots, almonds), soft fruit (gooseberries, currants, raspberries, blackberries), hard-shelled fruit (walnuts, hazelnuts, pecan nuts, pistachios), citrus fruits (oranges, grapefruits, mandarins, lemons), grapevines, figs, khaki plums, kiwi fruits, avocados, mangoes, lychees, dates and also coffee and cocoa, 5 however, prolonged constant yield is an essential economical factor so that variations in terms of quantity and quality of the products must be avoided as much as possible. Accordingly, biennial bearing induced by chemical growth regulators is economically unacceptable. 10 In HortScience 38 (2), pp. 293-298 (2003), D.C. Elfving, G.A. Lang and D.B. Visser describe that, in certain cherry varieties, treatment of the trees with a combination of prohexadione-calcium and ethephon leads to increased floral density combined with reduced vegetative growth. However, reduced flowering in the year following the treatment with prohexadione-calcium alone is not reported. 15 It is an object of the present invention to provide a growth-regulatory composition for the treatment of pome fruit which reduces the vegetative growth while simultaneously not substantially reducing floral development after the treatment. 20 Surprisingly, it has been found that ethephon prevents the phenomenon of reduced floral development which is found after pome fruit has been treated with certain acylcyclohexanedione derivatives. It has been found that this object can be achieved by the concomitant use of acylcyclohexanedione derivatives and ethephon. 25 The present invention therefore relates to the use of at least one compound of the formula I O 30
R
1 OOC- CO- R 2 (I) O 0 in which 35 R 1 is H or Cl-Co 10 -alkyl and
R
2 is Cl-Clo-alkyl or C 3 -Cl 10 -cycloalkyl, or salts thereof 40 together with 2-chloroethylphosphonic acid (ethephon), of the formula II O II
CICH
2 -CH----P-OH OH 45 (ll) 3 for the treatment of pome fruit, in particular for preventing the reduced floral development which is observed in pome fruit owing to treatment with acylcyclohexanedione derivatives of the formula I, and for preventing biennial bearing which may be induced by the treatment. 5 Pome fruit, for the purposes of the present invention is understood as meaning apples, pears or quinces, in particular apples or pears. The term pome fruit, or specified as apples, pears or quinces, refers to the fruit trees or plant parts thereof, but not to the fruits in harvested form. 10 The treatment is carried out in order to improve floral development in pome fruit. The improvement of floral development comprises in particular complete or at least partial prevention of the reduced floral development which can be attributed to treatment with acylcyclohexanedione derivatives. At the same time, the treatment should naturally 15 lead to reduced vegetative growth. "Complete or partial prevention of reduced floral development" means that, at a particular point in time or over the entire flowering season, plants treated in accordance with the invention have preferably at least 40%, especially preferably at least 60% and in particular at least 80% of the number of flowers, or, alternatively, the number of inflorescences, of untreated control plants, i.e. 20 control plants which have not been treated with growth regulators but exposed to otherwise identical conditions. The inflorescence is part of the shoot system of a number of Spermatophytes, such as pome fruit, which, as a rule, bears a multiplicity of flowers and later produces one or more fruits. 25 Partial or complete prevention of reduced floral development also exists when the plants which have been treated in accordance with the invention have, at a particular point in time or over the entire flowering season, significantly more flowers or, alternatively, inflorescences than plants which have been exposed to otherwise identical conditions but which have been treated exclusively with acylcyclohexanedione 30 derivatives, i.e. without ethephon. Acylcyclohexanedione compounds of the formula I are disclosed in EP-A 0 123 001 and EP-A 126 713. 35 The compounds of the formula I can be present not only in the trione form (triketo form) I.a, but also in the tautomeric keto-enol forms I.b and L.c, respectively: o OH O OH 40 R1OOC CO-R 2 R1OOC CO-R 2 - ROOC O R2 0 0 0 I.a I.b I.c 45 In the compounds of the formula I, R 1 is preferably H or C 1
-C
4 -alkyl.
4
R
2 preferably represents Cl-C 4 -alkyl or C 3
-C
6 -cycloalkyl and in particular ethyl or cyclopropyl. 5 In the definition of the radicals R 1 and R 2 , C 1 -Co 10 -alkyl is a linear or branched alkyl radical such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, neopentyl, hexyl, heptyl, octyl, 2-ethylhexyl, nonyl or decyl. C 1
-C
4 -alkyl is, for example, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl or tert-butyl. The alkyl radical is preferably linear. 10 In the definition of R 2 , C 3 -Cl 1 0 -cycloalkyl is, for example, cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl or decalin. C 3
-C
6 -Cycloalkyl is, for example, cyclopropyl, cyclopentyl or cyclohexyl. 15 The salts of the acylcyclohexanedione compounds I where R 1 # H are the salts of monoanions, while in the case of R 1 = H they may be the salts of the monoanions and of the dianions of these compounds. The monoanions can be present both as carboxylate anions I.d and as enolate anions I.e and I.f: 20 0 o e 0 eooc
CO-R
2 R'OOC
CO-R
2
R
1 OOCe
R
2 0 0 0 25 I.d I.e I.f Accordingly, the carboxylate and enolate groups are present together in the dianion. Preferred cations in the salts of the compounds of the formula I are the ions of the 30 alkali metals, preferably of lithium, sodium and potassium, of the alkaline earth metals, preferably of calcium and magnesium, and of the transition metals, preferably of manganese, copper, zinc and iron, furthermore ammonium (NH 4 ') and substituted ammonium where one to four hydrogen atoms are replaced by Cl-C 4 -alkyl, hydroxy Cl-C 4 -alkyl, C 1
-C
4 -alkoxy-Cl-C 4 -alkyl, hydroxy-C 1
-C
4 -alkoxy-Cl-C 4 -alkyl, phenyl or 35 benzyl, preferably ammonium, methylammonium, isopropylammonium, dimethylammonium, diisopropylammonium, trimethylammonium, tetrame-thylammo nium, tetraethylammonium, tetrabutylammonium, 2-hydroxyethylammonium, 2-(2-hydroxyeth-1l-oxy)eth-1-ylammonium, di(2-hydroxyeth-1-yl)ammonium, benzyltrimethylammonium, benzyltriethylammonium, moreover phosphonium ions, 40 sulfonium ions, preferably tri(Cl-C 4 -alkyl)sulfonium such as trimethylsulfonium and sulfoxonium ions, preferably tri(C 1
-C
4 -alkyl)sulfoxonium. Preferred cations are furthermore chlormequat [(2-chloroethyl)trimethylammonium], mepiquat (N,N-dimethyl piperidinium) and N,N-dimethylmorpholinium. Especially preferred cations are the alkali metal cations, the alkaline earth metal cations and the ammonium cation (NH 4 '). In 45 particular, the salt is the calcium salt.
5 For the purposes of the present invention, the term "compounds of the formula I" or "acylcyclohexanedione of the formula I" refers both to the neutral compounds I and to their salts. 5 Compounds I which are especially preferably used in accordance with the invention are prohexadione (R 1 = H, R 2 = ethyl), prohexadione-calcium (the calcium salt of prohexadione), trinexapac (R 1 = H, R 2 = cyclopropyl) and trinexapac-ethyl (R 1 = ethyl,
R
2 = cyclopropyl). 10 Pome fruit is preferably treated in such a way that the pome fruit tree, or plant parts thereof, is/are brought into contact with at least one acylcyclohexanedione compound I and ethephon. The compounds of the formula I and ethephon can be applied as mixture or separately. In the case of separate application, the individual active substances can be applied simultaneously or one after the other, preferably at an 15 interval of from a few hours up to several weeks in the case of successive application. The compounds I and ethephon are employed in a weight ratio of preferably from 10:1 to 1:5, especially preferably from 5:1 to 1:3, in particular of from 3:1 to 1:2. 20 The compounds of the formula I or their salts are preferably employed at an application rate of from 25 to 1 500 g/ha, especially preferably from 50 to 1 000 g/ha, per season. Prohexadione-calcium is employed in particular at an application rate of from 100 to 500 g/ha per season. Trinexapac-ethyl is employed at an application rate of, in particular, from 200 to 800 g/ha per season. Ethephon is preferably employed at an 25 application rate of from 25 to 1 500 g/ha, especially preferably from 50 to 750 g/ha and in particular from 100 to 500 g/ha per season. The active substances are preferably applied 1 to 5 times, especially preferably 1 to 4 times and in particular 2 to 3 times per season. 30 It is possible to employ the compound of the formula I together with ethephon in some of the applications only, and to use only one of the active substances, in particular the compound I, in the remaining applications. Preferably, both compound I and ethephon are used in at least half of the applications per season, especially preferably in half of 35 the applications per season and in particular in at least one application. The application timing, the number of applications and the application rates employed in each case depend on the fruit crop in question and on other parameters such as species and variety of the fruit, rootstock, age, weather conditions, availability of water 40 and nutrients, and must be specified in each individual case by the skilled worker. Application is preferably effected in spring to early summer (approximately beginning of March to end of July) in the northern hemisphere and, accordingly, from the beginning of September to the end of January in the southern hemisphere. In particular, the 45 treatment is effected when the new shoots start to grow anew, a point in time which generally correlates with the end of flowering or near this point in time, i.e. within ± 4 6 weeks. Further treatments can then follow within a period of up to 10 weeks, for example within 1 to 10 weeks after the first application. The timing of the treatment depends on the requirements of the crop plants in question, which may vary from season to season, depending on the weather conditions and the conditions of the 5 location. However, the skilled worker will be able to determine the treatment timings in the customary manner, and, as a rule, even treatment timings outside the intervals detailed herein are successful and may be meaningful, depending on the requirement of the crop plant. 10 The compounds of the formula I, ethephon or their mixture are typically employed as formulations as are customary in the field of crop protection. In the form of concentrated solutions, suspensions or emulsions, for example, they can be diluted with water and applied by spraying. The type of application depends on the 15 species and the variety of the pome fruit and on the plant part to which the mixtures are to be applied; in any case, they should ensure as fine as possible a distribution of the active ingredients and adjuvants. In addition to the compounds of the formula I and/or ethephon, the formulations may 20 comprise formulation auxiliaries which are conventionally used in the art of crop protection products, for example inert adjuvants and/or surface-active substances such as emulsifiers, dispersants, wetters and the like. Suitable surface-active substances are the alkali metal salts, alkaline earth metal salts 25 and ammonium salts of aromatic sulfonic acids, for example ligninsulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid and dibutylnaphthalenesulfonic acid, and of fatty acids, alkylsulfonates and alkylarylsulfonates, alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols and of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives 30 with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl ethers, tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene or polyoxypropylene alkyl ethers, 35 lauryl alcohol polyglycol ether acetate, sorbitol esters, lignin-sulfite waste liquors, methylcellulose or siloxanes. Examples of suitable siloxanes are polyether/polymethylsiloxane copolymers, which are also referred to as spreaders or penetrants. 40 Inert formulation auxiliaries which are suitable are essentially: mineral oil fractions of medium to high boiling point such as kerosine and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example paraffins, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols 45 such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone, strongly polar solvents, for example amines such as 7 N-methylpyrrolidone, and water. Aqueous use forms of the compounds I, of ethephon or of their mixture can be prepared from stock formulations such as emulsion concentrates, suspensions, pastes, 5 wettable powders or water-dispersible granules by addition of water. To prepare emulsions, pastes or oil dispersions, the compounds of the formula I or ethephon or their mixture, as such or in an oil or solvent, can be dissolved and homogenized in water by means of wetter, sticker, dispersant or emulsifier. Naturally, the use forms will comprise the adjuvants used in the stock formulations. 10 In a preferred embodiment, the compounds of the formula I, ethephon or their mixture are used in the form of an aqueous spray mixture. This spray mixture comprises the compounds of the formula I or ethephon in an amount of preferably in each case from 25 to 500 ppm. If the compounds of the formula I and ethephon are employed as a 15 mixture, the spray mixture comprises the active substances in a total amount of from preferably 50 to 1 000 ppm. The active ingredient combination of acylcyclohexanediones I and ethephon which is used in accordance with the invention can be used for application in all of the 20 abovementioned pome fruit species, but also in other plant species. Depending on the plant part to which it is to be applied, it can be applied using equipment which is known per se and conventionally used in agricultural practice, application in the form of an aqueous spray solution or spray mixture being preferred. 25 Application is preferably effected by spraying to run-off point. In this context, the mixture is applied either to all of the aerial plant part or else only to individual plant parts such as flowers, leaves or individual shoots. The choice of the individual plant parts which are to be treated depends on the plant species and its developmental stage. Preferably, all of the aerial part of the plant is treated. 30 Another subject matter of the present invention is a method for the treatment of pome fruit, which comprises applying at least one compound of the formula I and 2-chloroethylphosphonic acid (ethephon), as a mixture or separately, to pome fruit plants or parts of pome fruit plants in the form of an aqueous spray mixture either 35 simultaneously or in succession. The method is preferably employed for improving floral development. What has been said above regarding the compounds of the formula I and ethephon, 40 the aqueous composition and the application also applies analogously here. The flowering behavior of perennial pome fruit cultures in the year after the treatment is markedly improved by the use according to the invention of acylcyclohexanedione compounds I together with ethephon. In particular, the reduced floral development, 45 which can be attributed to the treatment with certain acylcyclohexanedione derivatives, 8 is essentially prevented. The desired growth regulation takes place simultaneously in the treated plants. The following examples are intended to illustrate the invention, but without imposing a 5 limitation.
9 Examples: 1. Flowering behavior in pears after treatment with prohexadione-calcium and ethephon 5 12-year-old pear trees cv. "Conference" on BA rootstock at two different locations were treated first with prohexadione-calcium alone and secondly with a combination of prohexadione-calcium and ethephon. To this end, 4 groups of 5 trees each, which were uniformly distributed in an orchard, were sprayed with an active-ingredient-comprising 10 spray mixture to run-off point (approx. 1 000 I/ha). Three applications at intervals of approximately one month were carried out at the first location. At the second location, prohexadione-calcium was applied four times to a part of the groups of trees and three times to another part, the application interval being in each case approximately two weeks. The combination of prohexadione-calcium and ethephon was applied twice, 15 with in each case one application with prohexadione-calcium alone being carried out before and after the combined application. Approximately one year after the first application, the number of inflorescences of untreated trees, of those which have been treated exclusively with prohexadione-calcium and of trees which had been treated with a combination of prohexadione-calcium and ethephon were counted and compared 20 with each other. The results are listed in Tables 1 and 2 hereinbelow.
10 Table 1: Location 1 Treatment Application timings 2002 and Total rate Flowering in the application rates of active [g/ha] subsequent year substance [g/ha] [number of inflorescences/tree] 15th 14th May 16th April 2003 April June Untreated - - - - 183 ProCa* 150 150 150 450 137 ProCa* + 150 150 150 450 185 ethephon 120 120 120 360 5 Table 2: Location 2 Treatment Application timings 2002 and Total Flowering in the application rates of active substance rate subsequent year [g/ha] [g/ha] [number of inflorescences/tree] 12th 3rd 15th 30th April 2003 April May May May Untreated - - - - - 250 ProCa* 120 87 87 95 389 157 ProCa* 120 87 87 - 294 152 ProCa* + 120 110 92 95 417 217 ethephon - 395 315 - 710 * Prohexadione-calcium 10 As can be seen from the above experimental results, the application of prohexadione calcium leads to reduced floral development in the year following the treatment. If, in contrast, prohexadione-calcium is applied in combination with ethephon, such a reduced floral development is either absent or markedly alleviated.
Claims (10)
1. The use of at least one compound of the formula I, 5 0O R 1 OOC C CO- R 2 (I) 0 10 in which R 1 is H or Cl-C 10 -alkyl and R 2 is C 1 -C 10 -alkyl or C 3 -Co 10 -cycloalkyl, 15 or salts thereof together with 2-chloroethylphosphonic acid (ethephon) for the treatment of pome fruit.
2. The use according to claim 1 for improving floral development. 20
3. The use according to any of the preceding claims for the treatment of apples or pears.
4. The use according to any of the preceding claims, where, in the compound of the formula I, R 1 is H and R 2 is ethyl and where the compound of the formula I in 25 which R 2 is ethyl is present in the form of the calcium salt.
5. The use according to any of claims 1 to 3, where, in the compound of the formula I, R 1 is ethyl and R 2 is cyclopropyl. 30
6. The use according to any of the preceding claims, wherein the compound of the formula I and 2-chloroethylphosphonic acid are employed in a weight ratio of from 10:1 to 1:5.
7. The use according to any of the preceding claims, wherein the compound of the 35 formula I and 2-chloroethylphosphonic acid are employed as a mixture in the form of an aqueous spray mixture in which the compound of the formula I and 2-chloroethylphosphonic acid are present in a total amount of from 50 to 1 000 ppm. 40
8. The use according to any of the preceding claims, wherein the application rate of the compound of the formula I and of 2-chloroethylphosphonic acid is in the range of from in each case 25 to 1 500 g/ha per season.
9. A method for the treatment of pome fruit, which comprises applying at least one 45 compound of the formula I and 2-chloroethylphosphonic acid, as a mixture or separately, to pome fruit plants or parts of pome fruit plants in the form of an 12 aqueous spray mixture, either simultaneously or in succession.
10. The method according to claim 9 for the treatment of pome fruit for improving floral development.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10336612 | 2003-08-08 | ||
| DE10336612.1 | 2003-08-08 | ||
| PCT/EP2004/008832 WO2005015997A1 (en) | 2003-08-08 | 2004-08-06 | Use of acyl cyclohexandione derivatives in conjunction with ethephon for treating pomaceous fruit |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004264668A1 true AU2004264668A1 (en) | 2005-02-24 |
| AU2004264668B2 AU2004264668B2 (en) | 2010-02-25 |
Family
ID=34177401
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004264668A Ceased AU2004264668B2 (en) | 2003-08-08 | 2004-08-06 | Use of acyl cyclohexandione derivatives in conjunction with ethephon for treating pomaceous fruit |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20060229208A1 (en) |
| EP (1) | EP1653805B2 (en) |
| JP (1) | JP4606412B2 (en) |
| KR (1) | KR20060063936A (en) |
| AR (1) | AR045346A1 (en) |
| AT (1) | ATE349160T1 (en) |
| AU (1) | AU2004264668B2 (en) |
| BR (1) | BRPI0413262A (en) |
| CA (1) | CA2534853A1 (en) |
| DE (1) | DE502004002479D1 (en) |
| ES (1) | ES2280044T5 (en) |
| MX (1) | MXPA06000935A (en) |
| NZ (1) | NZ544960A (en) |
| PL (1) | PL1653805T5 (en) |
| PT (1) | PT1653805E (en) |
| WO (1) | WO2005015997A1 (en) |
| ZA (1) | ZA200601925B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8580709B2 (en) * | 2009-11-27 | 2013-11-12 | Syngenta Crop Protection, Llc | Plant growth regulation |
| DK3578047T3 (en) | 2018-06-07 | 2022-12-19 | Fine Agrochemicals Ltd | Plant growth regulator system |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL29492A (en) * | 1967-02-23 | 1974-05-16 | Amchem Prod | Processes and compositions for the regulation of plant growth |
| US4374661A (en) * | 1967-12-27 | 1983-02-22 | Union Carbide Corporation | Growth regulation process |
| US4361436A (en) * | 1977-09-16 | 1982-11-30 | Gaf Corporation | Composition for plant growth regulation |
| DE2755940C2 (en) † | 1977-12-15 | 1986-01-02 | Basf Ag, 6700 Ludwigshafen | Means for regulating plant growth |
| JPS59196840A (en) * | 1983-04-22 | 1984-11-08 | Kumiai Chem Ind Co Ltd | Cyclohexane derivatives and plant growth regulators |
| DE3476195D1 (en) * | 1983-05-18 | 1989-02-23 | Ciba Geigy Ag | Cyclohexanedione-carboxylic-acid derivatives having a herbicidal and plant growth regulating activity |
| JP2673211B2 (en) * | 1988-05-19 | 1997-11-05 | クミアイ化学工業株式会社 | Plant growth regulating composition |
| ES2071079T3 (en) † | 1989-12-13 | 1995-06-16 | Ciba Geigy Ag | SYNERGETIC ACTION PRODUCTS AND PROCEDURE FOR THE REGULATION OF PLANT GROWTH. |
-
2004
- 2004-08-06 MX MXPA06000935A patent/MXPA06000935A/en active IP Right Grant
- 2004-08-06 EP EP04763867A patent/EP1653805B2/en not_active Expired - Lifetime
- 2004-08-06 BR BRPI0413262-9A patent/BRPI0413262A/en not_active Application Discontinuation
- 2004-08-06 PL PL04763867T patent/PL1653805T5/en unknown
- 2004-08-06 ES ES04763867T patent/ES2280044T5/en not_active Expired - Lifetime
- 2004-08-06 KR KR1020067002655A patent/KR20060063936A/en not_active Abandoned
- 2004-08-06 AT AT04763867T patent/ATE349160T1/en active
- 2004-08-06 US US10/567,467 patent/US20060229208A1/en not_active Abandoned
- 2004-08-06 AR ARP040102819A patent/AR045346A1/en unknown
- 2004-08-06 AU AU2004264668A patent/AU2004264668B2/en not_active Ceased
- 2004-08-06 PT PT04763867T patent/PT1653805E/en unknown
- 2004-08-06 JP JP2006522325A patent/JP4606412B2/en not_active Expired - Fee Related
- 2004-08-06 NZ NZ544960A patent/NZ544960A/en not_active IP Right Cessation
- 2004-08-06 CA CA002534853A patent/CA2534853A1/en not_active Abandoned
- 2004-08-06 WO PCT/EP2004/008832 patent/WO2005015997A1/en not_active Ceased
- 2004-08-06 DE DE502004002479T patent/DE502004002479D1/en not_active Expired - Lifetime
-
2006
- 2006-03-07 ZA ZA200601925A patent/ZA200601925B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL1653805T3 (en) | 2007-05-31 |
| AR045346A1 (en) | 2005-10-26 |
| ATE349160T1 (en) | 2007-01-15 |
| DE502004002479D1 (en) | 2007-02-08 |
| EP1653805B1 (en) | 2006-12-27 |
| PL1653805T5 (en) | 2012-01-31 |
| JP2007501772A (en) | 2007-02-01 |
| ZA200601925B (en) | 2007-05-30 |
| PT1653805E (en) | 2007-02-28 |
| JP4606412B2 (en) | 2011-01-05 |
| NZ544960A (en) | 2009-04-30 |
| KR20060063936A (en) | 2006-06-12 |
| AU2004264668B2 (en) | 2010-02-25 |
| US20060229208A1 (en) | 2006-10-12 |
| ES2280044T5 (en) | 2012-01-11 |
| CA2534853A1 (en) | 2005-02-24 |
| BRPI0413262A (en) | 2006-10-10 |
| EP1653805B2 (en) | 2011-08-17 |
| MXPA06000935A (en) | 2006-05-04 |
| WO2005015997A1 (en) | 2005-02-24 |
| EP1653805A1 (en) | 2006-05-10 |
| ES2280044T3 (en) | 2007-09-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US9295253B2 (en) | Use of abscisic acid on ornamental plants | |
| EP2282638B1 (en) | Method for improving the tolerance of crops to chilling temperatures and/or frost | |
| US8173577B2 (en) | Use of abscisic acid combinations for thinning | |
| EP2337453B1 (en) | Use of acylcyclohexanedione carboxylic acid or salts thereof in combination with acylcyclohexanedione carboxylic acid esters for improving the development of gramineous plants | |
| AU2004264668B2 (en) | Use of acyl cyclohexandione derivatives in conjunction with ethephon for treating pomaceous fruit | |
| EP2774484A1 (en) | Method for fruit thinning at late growth stages of fruit plants | |
| US8557736B2 (en) | Use of abscisic acid to control fruiting | |
| US7686975B2 (en) | Use of acylcyclohexanedione derivatives for improving the tolerance of plants to cold and/or frost | |
| DD254877A5 (en) | COMPOSITION AND METHOD FOR REGULATING PLANT GROWTH | |
| Palonen et al. | Growth control of “Glen Ample” and “Tulameen” raspberry cultivars with single and repeated ProCa applications | |
| DE2741343A1 (en) | AGENTS FOR REGULATING PLANT GROWTH |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |